Banking Client Partner - Toronto

hire dig italent; Toronto; On-site; CAD 70,000 - 85,000; Full time

Job summary

hire dig italent is seeking a Lead/Senior Consultant in GMP Quality Assurance for pharmaceutical projects. The role focuses on applying GMP knowledge to deviations, CAPA, change controls, audits, and batch release within a team environment.

Eligible candidates will have 4–7 years of experience in quality and compliance for health products, with a Bachelor’s degree and willingness for on-site engagements. CAD salary range is provided.

Qualifications

• Importation experience and knowledge of GMP compliance.
• Change management and deviation investigations experience.
• Master manufacturing/batch record review and lot release knowledge.
• Annual Product Quality Reviews familiarity.
• Stability review and assessment experience.

Responsibilities

• Establishing project plans that capture all aspects of the scope of work.
• Prioritizing and managing compliance projects.
• Completing critical assessments of data and documents to identify gaps.
• Communicating project milestones on a monthly basis.
• Completing client assigned tasks: deviation investigations, management of quality systems, review of documentation.
• Developing documentation as required by the project: SOPs, protocols, reports, etc.
• Conducting audits both internal and external.
• Releasing product to market.

Skills

Importation

Change Management

Deviation investigations

Batch record review

Annual Product Quality Reviews

Stability review

Education

Bachelor's degree

Job description

This Pharmaceutical Consulting role focuses on applying your GMP knowledge and experience to various projects, such that the client is confident in the approach and timing of execution of the project. Our consultants work independently within a team environment to ensure activities are undertaken in a timely manner. This position may require onsite consultant engagements within the pharmaceutical industry.

We are looking for consultants who want to apply their in‑depth quality and compliance knowledge and out‑of‑the‑box thinking to challenging projects with our clients. Our projects cover, but are not limited to: deviation investigations, change controls, CAPA, auditing, management of quality systems, delivery of training, batch document review, imported product disposition, related to pharmaceuticals, biologics, NHPs and Medical Devices. The successful candidate would be placed in the GMP Consulting operational team who support various quality consulting roles.

In this broad‑based role, you will support the projects assigned to you, meeting the client’s needs. The role specifically prioritizes, plans, organizes and executes projects related to quality and compliance of health products to ensure smooth implementations. The role may involve coordinating/working with client personnel to meet project goals.

Reporting to the VP Consulting Services, the Lead/Senior Consultant is responsible for:

• Establishing project plans that capture all aspects of the scope of work
• Prioritizing and managing compliance projects
• Completing critical assessments of data and documents to identify gaps compared to regulatory requirements
• Communicating project milestones on a monthly basis
• Completing client assigned tasks: deviation investigations, management of quality systems, review of documentation
• Developing documentation as required by the project: SOPs, protocols, reports, etc.
• Conducting audits both internal and external
• Releasing product to market

If you are a Quality Assurance professional in the Pharmaceutical industry with at least 4-7 years experience, we have the environment and exposure to the type of work you want to do.

Requirements

Education - Bachelors' degree required

Experience in the following is required:

• Importation
• Change Management
• Deviation investigations
• Master manufacturing/batch record review and lot release
• Annual Product Quality Reviews
• Stability review and assessment

Salary range: CAD 70,000 – 85,000 annually

Annual salary will be based on candidate’s experience, skill, knowledge, and qualifications relevant to the role.

This posting is for an existing vacancy.

Q&C welcomes and encourages applications from people with disabilities. Accommodations are available on request for candidates taking part in all aspects of the selection process